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Name Date Date initiated Country Source
Recall of VACLOCK Syringe 2010-10-22 United States USFDA
Recall of VACLOCK Syringe 2010-10-22 United States USFDA
Recall of Elekta VBH Head FIX 2010-10-14 United States USFDA
Recall of MEDALLION Syringe 2010-10-22 United States USFDA
Recall of Merit Custom Kits 2010-10-25 United States USFDA
Recall of MEDALLION Syringe 2010-10-22 United States USFDA
Recall of Protg "GPS" SelfExpanding Biliary Stent System 2010-10-30 United States USFDA
Recall of 3M ESPE Stainless Steel Primary Molar Crowns 2010-10-06 United States USFDA
Recall of Rectal Tubes 22 French/20 French 2010-10-28 United States USFDA
Recall of Edwards Protection Cannulae Monitoring and Infusion Set 2010-10-19 United States USFDA
Recall of Edwards Protection Cannulae Monitoring and Infusion Set 2010-10-19 United States USFDA
Recall of Philips HeartStart FR2 AED with Text Display , Model M3861 2010-09-22 United States USFDA
Recall of HeartStart FR2 AED with ECG Display, Model 3840, Laerdal Brand 2010-09-22 United States USFDA
Recall of HeartStart FR2 AED with Text Display, Model 3841, Laerdal brand 2010-09-22 United States USFDA
Recall of HeartStart FR2 AED with ECG Display, Model 989803148601 2010-09-22 United States USFDA
Recall of Zimmer NexGen LPS 2010-09-15 United States USFDA
Recall of HeartStart FR2 AED with ECG Display, Model 989803148611 2010-09-22 United States USFDA
Recall of SODASORB LF PrePaks 2010-10-20 United States USFDA
Recall of Penumbra System Reperfusion Catheter 032 2010-10-25 United States USFDA
Recall of Merit Custom Kits 2010-10-25 United States USFDA
Recall of Merit Custom Kits 2010-10-25 United States USFDA
Recall of Merit Custom Kits 2010-10-25 United States USFDA
Recall of Merit Custom Kits 2010-10-25 United States USFDA
Recall of Merit Custom Kits 2010-10-25 United States USFDA
Recall of Merit Custom Kits 2010-10-25 United States USFDA